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The Microbiota of Breast Tissue and Its Association with Breast Cancer

In the United States, 1 in 8 women will be diagnosed with breast cancer in her lifetime. Along with genetics, the environment contributes to disease development, but what these exact environmental factors are remains unknown. We have previously shown that breast tissue is not sterile but contains a...

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Autores principales: Urbaniak, Camilla, Gloor, Gregory B., Brackstone, Muriel, Scott, Leslie, Tangney, Mark, Reid, Gregor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968547/
https://www.ncbi.nlm.nih.gov/pubmed/27342554
http://dx.doi.org/10.1128/AEM.01235-16
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author Urbaniak, Camilla
Gloor, Gregory B.
Brackstone, Muriel
Scott, Leslie
Tangney, Mark
Reid, Gregor
author_facet Urbaniak, Camilla
Gloor, Gregory B.
Brackstone, Muriel
Scott, Leslie
Tangney, Mark
Reid, Gregor
author_sort Urbaniak, Camilla
collection PubMed
description In the United States, 1 in 8 women will be diagnosed with breast cancer in her lifetime. Along with genetics, the environment contributes to disease development, but what these exact environmental factors are remains unknown. We have previously shown that breast tissue is not sterile but contains a diverse population of bacteria. We thus believe that the host's local microbiome could be modulating the risk of breast cancer development. Using 16S rRNA amplicon sequencing, we show that bacterial profiles differ between normal adjacent tissue from women with breast cancer and tissue from healthy controls. Women with breast cancer had higher relative abundances of Bacillus, Enterobacteriaceae and Staphylococcus. Escherichia coli (a member of the Enterobacteriaceae family) and Staphylococcus epidermidis, isolated from breast cancer patients, were shown to induce DNA double-stranded breaks in HeLa cells using the histone-2AX (H2AX) phosphorylation (γ-H2AX) assay. We also found that microbial profiles are similar between normal adjacent tissue and tissue sampled directly from the tumor. This study raises important questions as to what role the breast microbiome plays in disease development or progression and how we can manipulate this for possible therapeutics or prevention. IMPORTANCE This study shows that different bacterial profiles in breast tissue exist between healthy women and those with breast cancer. Higher relative abundances of bacteria that had the ability to cause DNA damage in vitro were detected in breast cancer patients, as was a decrease in some lactic acid bacteria, known for their beneficial health effects, including anticarcinogenic properties. This study raises important questions as to the role of the mammary microbiome in modulating the risk of breast cancer development.
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spelling pubmed-49685472016-08-08 The Microbiota of Breast Tissue and Its Association with Breast Cancer Urbaniak, Camilla Gloor, Gregory B. Brackstone, Muriel Scott, Leslie Tangney, Mark Reid, Gregor Appl Environ Microbiol Microbial Ecology In the United States, 1 in 8 women will be diagnosed with breast cancer in her lifetime. Along with genetics, the environment contributes to disease development, but what these exact environmental factors are remains unknown. We have previously shown that breast tissue is not sterile but contains a diverse population of bacteria. We thus believe that the host's local microbiome could be modulating the risk of breast cancer development. Using 16S rRNA amplicon sequencing, we show that bacterial profiles differ between normal adjacent tissue from women with breast cancer and tissue from healthy controls. Women with breast cancer had higher relative abundances of Bacillus, Enterobacteriaceae and Staphylococcus. Escherichia coli (a member of the Enterobacteriaceae family) and Staphylococcus epidermidis, isolated from breast cancer patients, were shown to induce DNA double-stranded breaks in HeLa cells using the histone-2AX (H2AX) phosphorylation (γ-H2AX) assay. We also found that microbial profiles are similar between normal adjacent tissue and tissue sampled directly from the tumor. This study raises important questions as to what role the breast microbiome plays in disease development or progression and how we can manipulate this for possible therapeutics or prevention. IMPORTANCE This study shows that different bacterial profiles in breast tissue exist between healthy women and those with breast cancer. Higher relative abundances of bacteria that had the ability to cause DNA damage in vitro were detected in breast cancer patients, as was a decrease in some lactic acid bacteria, known for their beneficial health effects, including anticarcinogenic properties. This study raises important questions as to the role of the mammary microbiome in modulating the risk of breast cancer development. American Society for Microbiology 2016-07-29 /pmc/articles/PMC4968547/ /pubmed/27342554 http://dx.doi.org/10.1128/AEM.01235-16 Text en Copyright © 2016 Urbaniak et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Microbial Ecology
Urbaniak, Camilla
Gloor, Gregory B.
Brackstone, Muriel
Scott, Leslie
Tangney, Mark
Reid, Gregor
The Microbiota of Breast Tissue and Its Association with Breast Cancer
title The Microbiota of Breast Tissue and Its Association with Breast Cancer
title_full The Microbiota of Breast Tissue and Its Association with Breast Cancer
title_fullStr The Microbiota of Breast Tissue and Its Association with Breast Cancer
title_full_unstemmed The Microbiota of Breast Tissue and Its Association with Breast Cancer
title_short The Microbiota of Breast Tissue and Its Association with Breast Cancer
title_sort microbiota of breast tissue and its association with breast cancer
topic Microbial Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968547/
https://www.ncbi.nlm.nih.gov/pubmed/27342554
http://dx.doi.org/10.1128/AEM.01235-16
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